يعرض 1 - 5 نتائج من 5 نتيجة بحث عن '"Lydia Mare"', وقت الاستعلام: 1.28s تنقيح النتائج
  1. 1
    Cytogenetic monitoring in Shwachman-Diamond syndrome: a note on clonal progression and a practical warning

    المؤلفون: Giuseppe Montalbano, Emanuela Maserati, Barbara Pressato, Francesco Pasquali, Francesco Lo Curto, Roberto Valli, Cristina Marletta, Lydia Mare

    المصدر: Journal of pediatric hematology/oncology. 37(4)

    مصطلحات موضوعية: Chromosome Aberrations, Shwachman–Diamond syndrome, Pathology, medicine.medical_specialty, business.industry, cytogenetic monitoring, Chromosomes, Human, Pair 20, Chromosome, Hematology, Disease, medicine.disease, Shwachman-Diamond Syndrome, medicine.anatomical_structure, chromosome anomalies, Oncology, Pediatrics, Perinatology and Child Health, medicine, Humans, Lipomatosis, Exocrine Pancreatic Insufficiency, Bone marrow, business, Bone Marrow Diseases, Chromosomes, Human, Pair 7, Shwachman-Diamond syndrome, chromosome anomalies, cytogenetic monitoring

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43c7b5447bd9f27f99cbb9f47930f5edTest
    https://pubmed.ncbi.nlm.nih.gov/25887640Test


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  2. 2
    Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes

    المؤلفون: Lydia Mare, Giuseppe Loffredo, Maria Ester Bernardo, Marco Zecca, Roberto Valli, Alessandra Di Cesare-Merlone, Barbara Pressato, Luciana Vinti, Emanuela Maserati, Giuseppe Montalbano, Cristina Marletta, Franco Locatelli, Giuseppe Menna, Francesco Pasquali, Simona Ferrari, Francesco Lo Curto

    المساهمون: Marletta, C., Valli, R., Pressato, B., Mare, L., Montalbano, G., Menna, G., Loffredo, G., Bernardo, M. E., Vinti, L., Ferrari, S., Di Cesare-Merlone, A., Zecca, M., Lo Curto, F., Locatelli, F., Pasquali, F., Maserati, E.

    المصدر: Molecular Cytogenetics, Vol 5, Iss 1, p 39 (2012)
    Molecular Cytogenetics

    مصطلحات موضوعية: medicine.medical_specialty, RUNX1, lcsh:QH426-470, MPL, Biochemistry, chemistry.chemical_compound, Chromosome structural anomalies, hemic and lymphatic diseases, Genetics, medicine, Genetics(clinical), Molecular Biology, Genetics (clinical), Biochemistry, medical, Cytopenia, business.industry, Research, Biochemistry (medical), Cytogenetics, Chromosome 1, Chromosome, medicine.disease, Thrombocytopenia, SAA, Human genetics, Peripheral, Chromosome 21, lcsh:Genetics, medicine.anatomical_structure, chemistry, Immunology, CAMT, Molecular Medicine, Bone marrow, business

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de660cac88b5a8840648876e2ccf1e44Test
    https://doi.org/10.1186/1755-8166-5-39Test


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  3. 3
    Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis

    المؤلفون: Francesco Pasquali, Emanuela Maserati, Roberto Valli, Francesco Lo Curto, Barbara Pressato, Giuseppe Montalbano, Lydia Mare, Cristina Marletta

    المصدر: British journal of haematology. 157(4)

    مصطلحات موضوعية: Pathology, medicine.medical_specialty, Chromosomes, Human, Pair 20, Biology, Bone Marrow, medicine, Humans, Lipomatosis, Eukaryotic Initiation Factors, Gene, Bone Marrow Diseases, centromere structure, Shwachman–Diamond syndrome, Hematology, medicine.disease, Prognosis, Shwachman-Diamond Syndrome, medicine.anatomical_structure, Shwachman-Diamond Syndrome, isochromosome i(7)(q10), centromere structure, EIF6, Cancer research, Exocrine Pancreatic Insufficiency, Bone marrow, Chromosome 20, isochromosome i(7)(q10), Chromosome Deletion

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::117c6e25dc4b51c1f1d357c143b3dbb6Test
    https://pubmed.ncbi.nlm.nih.gov/22295858Test


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  4. 4
    Clonal chromosome anomalies affecting FLI1 mimic inherited thrombocytopenia of the Paris-Trousseau type

    المؤلفون: Alessandro Pecci, Lydia Mare, Patrizia Noris, Roberto Valli, Carlo L. Balduini, Cristina Marletta, Rosangela Invernizzi, Emanuela Maserati

    المصدر: Europe PubMed Central

    مصطلحات موضوعية: Adult, Pathology, medicine.medical_specialty, Megakaryocyte differentiation, Locus (genetics), Chromosomal translocation, Biology, Contiguous gene syndrome, Thrombocytopenia Paris-Trousseau type, medicine, cquired thrombocytopenia, FLI1, Thrombocytopenia Paris-Trousseau type, Humans, Jacobsen Distal 11q Deletion Syndrome, Chromosome Aberrations, cquired thrombocytopenia, Proto-Oncogene Protein c-fli-1, FLI1, Chromosome, Hematology, General Medicine, medicine.disease, medicine.anatomical_structure, Immunology, Female, Bone marrow, Comparative genomic hybridization

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c233794036021f79bb97ee578c57069Test
    http://europepmc.org/abstract/med/22775407Test


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  5. 5
    Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms

    المؤلفون: Francesco Pasquali, Giuseppe Montalbano, Roberto Valli, Cristina Marletta, Barbara Pressato, Francesco Lo Curto, Emanuela Maserati, Lydia Mare

    المصدر: Molecular Cytogenetics

    مصطلحات موضوعية: medicine.medical_specialty, Myeloid, Biochemistry, hemic and lymphatic diseases, del(20)(q), medicine, Genetics, Genetics(clinical), Molecular Biology, Genetics (clinical), Biochemistry, medical, Shwachman–Diamond syndrome, business.industry, Shwachman-Diamond syndrome, Myeloid neoplams, Myelodysplastic syndromes, Research, Biochemistry (medical), Breakpoint, Cytogenetics, Myeloid leukemia, medicine.disease, medicine.anatomical_structure, Cancer research, Molecular Medicine, Chromosome 20, business, Comparative genomic hybridization

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41e8511e364dc51981d6f4fee0c32ceaTest


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